SI1403277T1 - Method for synthesis of (2S,3aS,7aS)-1-((S)-alanyl)-octahydro-1H-indole-2-carboxylic acid derivatives and use in the synthesis of perindopril - Google Patents
Method for synthesis of (2S,3aS,7aS)-1-((S)-alanyl)-octahydro-1H-indole-2-carboxylic acid derivatives and use in the synthesis of perindoprilInfo
- Publication number
- SI1403277T1 SI1403277T1 SI200330092T SI200330092T SI1403277T1 SI 1403277 T1 SI1403277 T1 SI 1403277T1 SI 200330092 T SI200330092 T SI 200330092T SI 200330092 T SI200330092 T SI 200330092T SI 1403277 T1 SI1403277 T1 SI 1403277T1
- Authority
- SI
- Slovenia
- Prior art keywords
- synthesis
- perindopril
- alanyl
- octahydro
- indole
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
- C07K5/022—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -X-C(=O)-(C)n-N-C-C(=O)-Y-; X and Y being heteroatoms; n being 1 or 2
- C07K5/0222—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -X-C(=O)-(C)n-N-C-C(=O)-Y-; X and Y being heteroatoms; n being 1 or 2 with the first amino acid being heterocyclic, e.g. Pro, Trp
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
- C07K5/06026—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atom, i.e. Gly or Ala
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Cardiology (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Indole Compounds (AREA)
- Catalysts (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP03290486A EP1403277B1 (en) | 2003-02-28 | 2003-02-28 | Method for synthesis of (2S,3aS,7aS)-1-((S)-alanyl)-octahydro-1H-indole-2-carboxylic acid derivatives and use in the synthesis of perindopril |
Publications (1)
Publication Number | Publication Date |
---|---|
SI1403277T1 true SI1403277T1 (en) | 2005-12-31 |
Family
ID=31970534
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SI200330092T SI1403277T1 (en) | 2003-02-28 | 2003-02-28 | Method for synthesis of (2S,3aS,7aS)-1-((S)-alanyl)-octahydro-1H-indole-2-carboxylic acid derivatives and use in the synthesis of perindopril |
Country Status (19)
Country | Link |
---|---|
US (1) | US7157485B2 (en) |
EP (1) | EP1403277B1 (en) |
JP (1) | JP4279871B2 (en) |
CN (1) | CN1331883C (en) |
AR (1) | AR043410A1 (en) |
AT (1) | ATE305939T1 (en) |
AU (1) | AU2004218202B2 (en) |
DE (1) | DE60301774T2 (en) |
DK (1) | DK1403277T3 (en) |
EA (1) | EA009062B1 (en) |
ES (1) | ES2249691T3 (en) |
HK (1) | HK1086280A1 (en) |
MY (1) | MY136851A (en) |
NZ (1) | NZ541423A (en) |
PL (1) | PL211506B1 (en) |
PT (1) | PT1403277E (en) |
SI (1) | SI1403277T1 (en) |
WO (1) | WO2004078708A2 (en) |
ZA (1) | ZA200505780B (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SI1403277T1 (en) * | 2003-02-28 | 2005-12-31 | Servier Lab | Method for synthesis of (2S,3aS,7aS)-1-((S)-alanyl)-octahydro-1H-indole-2-carboxylic acid derivatives and use in the synthesis of perindopril |
ES2250847T3 (en) * | 2003-02-28 | 2006-04-16 | Les Laboratoires Servier | NEW ACID SYNTHESIS PROCEDURE (2S, 3AS, 7AS) -PERHYDROINDOL-2-CARBOXYL AND ITS ETERES AND ITS APPLICATION TO PERINDROPIL SYNTHESIS. |
EP2200981B1 (en) | 2007-10-17 | 2011-12-07 | DSM IP Assets B.V. | Novel carbamoylglycine derivatives |
WO2009098251A1 (en) * | 2008-02-07 | 2009-08-13 | Dsm Ip Assets B.V. | NOVEL CYCLOALKANONE β-SUBSTITUTED ALANINE DERIVATIVES |
WO2011133651A1 (en) * | 2010-04-20 | 2011-10-27 | Chiral Quest , Inc. | An enantioselective process for cycloalkenyl b-substituted alanines |
CN106657507B (en) * | 2015-11-03 | 2019-07-02 | 中移(杭州)信息技术有限公司 | A kind of acoustic echo removing method and device |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IE55867B1 (en) * | 1981-12-29 | 1991-02-14 | Hoechst Ag | New derivatives of bicyclic aminoacids,processes for their preparation,agents containing these compounds and their use,and new bicyclic aminoacids as intermediates and processes for their preparation |
NL1008302C2 (en) * | 1998-02-13 | 1999-08-16 | Dsm Nv | Process for the preparation of an optically active indoline-2-carboxylic acid or derivative thereof. |
US6433153B1 (en) * | 1999-09-02 | 2002-08-13 | Lexicon Genetics Incorporated | Human calcium dependent proteases and polynucleotides encoding the same |
FR2807431B1 (en) * | 2000-04-06 | 2002-07-19 | Adir | NOVEL PROCESS FOR THE SYNTHESIS OF PERINDOPRIL AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS |
FR2827860B1 (en) * | 2001-07-24 | 2004-12-10 | Servier Lab | NOVEL PROCESS FOR SYNTHESIS OF ACID DERIVATIVES (2S, 3AS, 7AS) -1 - [(S) -ALANYL] -OCTAHYDRO-1H-INDOLE-2-CARBOXYLINE AND APPLICATION TO THE SYNTHESIS OF PERINDOPRIL |
SI1403277T1 (en) * | 2003-02-28 | 2005-12-31 | Servier Lab | Method for synthesis of (2S,3aS,7aS)-1-((S)-alanyl)-octahydro-1H-indole-2-carboxylic acid derivatives and use in the synthesis of perindopril |
-
2003
- 2003-02-28 SI SI200330092T patent/SI1403277T1/en unknown
- 2003-02-28 AT AT03290486T patent/ATE305939T1/en active
- 2003-02-28 DK DK03290486T patent/DK1403277T3/en active
- 2003-02-28 ES ES03290486T patent/ES2249691T3/en not_active Expired - Lifetime
- 2003-02-28 PT PT03290486T patent/PT1403277E/en unknown
- 2003-02-28 DE DE60301774T patent/DE60301774T2/en not_active Expired - Lifetime
- 2003-02-28 EP EP03290486A patent/EP1403277B1/en not_active Expired - Lifetime
-
2004
- 2004-02-27 NZ NZ541423A patent/NZ541423A/en not_active IP Right Cessation
- 2004-02-27 JP JP2006500162A patent/JP4279871B2/en not_active Expired - Fee Related
- 2004-02-27 PL PL377220A patent/PL211506B1/en unknown
- 2004-02-27 EA EA200501257A patent/EA009062B1/en not_active IP Right Cessation
- 2004-02-27 WO PCT/FR2004/000445 patent/WO2004078708A2/en active Application Filing
- 2004-02-27 US US10/547,132 patent/US7157485B2/en not_active Expired - Fee Related
- 2004-02-27 AR ARP040100610A patent/AR043410A1/en not_active Application Discontinuation
- 2004-02-27 MY MYPI20040681A patent/MY136851A/en unknown
- 2004-02-27 ZA ZA200505780A patent/ZA200505780B/en unknown
- 2004-02-27 AU AU2004218202A patent/AU2004218202B2/en not_active Ceased
- 2004-02-27 CN CNB2004800054063A patent/CN1331883C/en not_active Expired - Fee Related
-
2006
- 2006-05-29 HK HK06106194A patent/HK1086280A1/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
EP1403277A1 (en) | 2004-03-31 |
DK1403277T3 (en) | 2005-11-21 |
ATE305939T1 (en) | 2005-10-15 |
AR043410A1 (en) | 2005-07-27 |
CN1753907A (en) | 2006-03-29 |
PT1403277E (en) | 2005-11-30 |
US20060149082A1 (en) | 2006-07-06 |
WO2004078708A3 (en) | 2004-10-14 |
ZA200505780B (en) | 2006-09-27 |
EA009062B1 (en) | 2007-10-26 |
JP2006519176A (en) | 2006-08-24 |
AU2004218202A1 (en) | 2004-09-16 |
AU2004218202B2 (en) | 2009-07-30 |
EP1403277B1 (en) | 2005-10-05 |
WO2004078708A2 (en) | 2004-09-16 |
CN1331883C (en) | 2007-08-15 |
US7157485B2 (en) | 2007-01-02 |
HK1086280A1 (en) | 2006-09-15 |
PL211506B1 (en) | 2012-05-31 |
JP4279871B2 (en) | 2009-06-17 |
ES2249691T3 (en) | 2006-04-01 |
MY136851A (en) | 2008-11-28 |
DE60301774D1 (en) | 2006-02-16 |
EA200501257A1 (en) | 2006-04-28 |
PL377220A1 (en) | 2006-01-23 |
DE60301774T2 (en) | 2006-07-20 |
NZ541423A (en) | 2008-03-28 |
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